Colon Cancer: Gene >> SSPN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000242729
Start	26230801:26230801(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.457T>C
AA Mutation	p.Phe153Leu(p.F153L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000242729
Start	26230865:26230865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.521G>T
AA Mutation	p.Arg174Met(p.R174M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242729
Start	26195870:26195870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747147935
CDS Mutation	c.198C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242729
Start	26224370:26224370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.357T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242729
Start	26231046:26231046(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs543594167
CDS Mutation	c.702G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SSPN

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242729
Start	26230755:26230755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.411G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242729
Start	26230821:26230821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779535775
CDS Mutation	c.477C>T
Mutation Classification	Silent
Feature Type	Transcript